
Thermo Fisher Scientific NIPA2 Polyclonal Antibody
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Applications
Tested Dilution
Publications
Western Blot (WB)
0.04-0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC (P))
1:500-1:1,000
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant protein corresponding to Human NIPA2. Recombinant protein control fragment (Product #RP-104121). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
NIPA2,
uniProtId:
Q8N8Q9-1,
ncbiNodeId:
9606,
antigenRange:
132-154,
antigenLength:
360,
antigenImageFileName:
PA5-64313_NIPA2_Q8N8Q9-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-64313_NIPA2_Q8N8Q9-1_Rabbit_PDP.jpeg,
sortOrder:
2}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.4 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
PBS, pH 7.2, with 40% glycerol
Contains
0.02% sodium azide
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Wet ice
RRID
AB_2644686
Product Specific Information
Immunogen sequence: KEEEIETLNE MSHKLGDPGF VVF
Highest antigen sequence identity to the following orthologs: Mouse - 100%, Rat - 100%.
Target Information
Nipa2 encodes a protein that acts as a selective Mg(2+) transporter. The Nipa2 gene encodes a possible magnesium transporter, and is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing of the Nipa2 gene results in multiple transcript variants. Pseudogenes of the Nipa2 gene are found on chromosomes 3, 7 and 21. Diseases associated with NIPA2 include Angelman Syndrome and Prader-Willi Syndrome.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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